Average salary: $137,929 /yearly
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- Overview Clinical SAS Programmer job at cGxPServe. Princeton, NJ. Responsibilities Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s). Produces and delivers CDISC and regulatory compliant SDTM,...SAS
- Clinical SAS Programmer Job Summary: We're looking for an experienced Clinical SAS Programmer to lead statistical programming activities related to the development and maintenance of integrated clinical safety datasets across one or more compounds, indications, or therapeutic...SASContract workRemote work
- ...CDISC CDASH and SDTM conformant elements. Write and manage SAS code for mapping clinical data to SDTM data structures in conformance with Emme's... ...in developing technical documentation. SAS Certified Base Programmer certification required. Experience with development,...SAS
$60 - $80 per hour
...closely with Data Management and cross-functional teams to generate clinical trial metrics, support data cleaning and reconciliation... ...team PREFERRED Qualifications: Experience with Python and/or SAS in a clinical programming context Experience generating CDISC...SASContract workRemote work- Sr. Clinical SAS Programmer job at cGxPServe. Newark, NJ. Responsibilities: Perform data manipulation, analysis, and reporting of clinical trial data. Develop and maintain department/system-level macros. Create and review SDTM and ADaM specifications. Create and validate...SAS
- ...produced a diverse pipeline of commercial, clinical and preclinical candidates that have well... ...with genetic diseases. Senior Clinical Programmer - Summary The Senior Clinical Programmer... ...execute data quality checks; convert to SAS datasets; check for patient ID; ensure review...SASWorldwide
- ...positions from our partner companies. Job descriptions: Senior SAS Programmer Senior Statistical Programmer * -Perform SAS data... ...and analysis programming -May work with medical writing, clinical operations, and other clinical staff to support deliverables....SASFull time
Wizsolution
Plainsboro, NJ16 days ago - ...role in driving data integrity and analytical excellence across clinical development programs. The group fosters a collaborative and innovation... ...and Biostatistics teams. Build and maintain robust SAS macros and utilities to optimize workflows. Ensure quality, consistency...SASFull timeContract work
Axiom Path
Bridgewater, NJ3 days ago - Mandatory: SDTM, SAS Looking for 5+ years of clinical SAS programmers having in depth knowledge of CDISC SDTM. Gathering data from all available sources and using SAS to process it. Creating and writing programs. Preparing and presenting operations reports to the management...SAS
- Responsibilities Develop SAS coding for generating SDTM, ADaM datasets and TLFs to support clinical study analysis. Review and ensure accurate and high-quality statistical programming deliverables from CRO. Perform generation, validation and QC/QA of SDTM, ADaM and TLF...SAS
- ...while securing top talent. Qualifications Performs all SAS programming required for clinical trial analysis and reporting. Ensures activities and... ...guidance of the project statistician. Acts as the primary programmer to produce tables, listings, and figures for the...SAS
- Join to apply for the SAS Programmer role at Katalyst CRO . Overview Responsibilities Develop and validate programs that create datasets... ...study complexity, ensuring adherence to ICH guidelines, Good Clinical Practices, and regulatory requirements. Mentor junior programmers...SASFull timeContract work
- Overview Senior SAS Developer (Contract) based in Omaha, NE. The following responsibilities and qualifications describe the expected... ...Perform data manipulation, analysis and reporting of primarily clinical trial data. Create SDTM datasets. Create analysis datasets. Program...SASContract work
- Join to apply for the SAS Programmer role at Katalyst CRO Overview The statistical programming contractor independently manages completed... ...inputs to design and analysis, and reporting the results of clinical trials, including programming rules and mocked T/L/G. In addition...SASContract workFor contractorsWork experience placement
- ...rapidly, and we are currently seeking a full-time, office-based SAS Programmer to join our Biostatistics team. This position will work on a... ...Minimum 3.4 GPA Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV...SASFull timeContract workWork at officeLocal area
- ...variable cost. Job Description The Statistical Programmer is responsible for providing significant... ...and figures) and reporting of results of clinical studies. It includes Safety,... ...implementing new standards. Skills: Knowledge of SAS software, including macros programs development...SASImmediate start
- Join to apply for the SAS Programmer role at Katalyst CRO Overview The statistical programming contractor independently manages completed... ...providing inputs to design and analysis, reporting the results of clinical trials, and providing programming support for publications...SASContract workFor contractorsWork experience placement
- ...Perform data manipulation, analysis and reporting of primarily clinical trial data. Create analysis data sets (ADaM & SDTM). Program and... ...generate tables, listings and graphs (TLGs). Validate and document SAS programs and output. Fulfill ad-hoc analysis requests. Other...SASFull time
$65 - $71.8 per hour
...accurate execution of programming components of clinical trials. The statistical programming... ...-submission. Develop, debug, and enhance SAS programs to support quality control of... ...pharmaceutical or clinical research setting as a programmer. • Proficient knowledge of clinical...SASRemote jobContract workFor contractorsWork experience placement- ...rapidly, and we are currently seeking a full-time, office-based SAS Programmer to join our Biostatistics team. This position will work on a... ...GPA of 3.4. Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical...SASFull timeContract workWork at officeLocal areaImmediate startFlexible hours
- ...summary: The role of the Senior Statistical Programmer is to perform statistical programming activities for all assigned Phase I-IV clinical studies. This includes statistical... ...experience in statistical programming with SAS in a pharmaceutical or CRO environment. •...SASPermanent employment
- ...and maintain supporting documentation. Demonstrable expertise in SAS analysis and reporting programming. Demonstrable expertise with... ...mathematics, or life science. A minimum of 5 years of relevant clinical research programming experience, 3 years specifically in the pharmaceutical...SAS
- Overview Sr. SAS Programmer role at Katalyst CRO . Responsibilities Prepare data for state-of-the-art analysis, such as PPK, PKPD, exposure... ..., and regulatory drug submissions. General knowledge of clinical drug development and demonstrated knowledge of pharmacokinetics...SASContract work
- ...customers. Qualifications At least 2 years of work experience using SAS in the data review, analysis and/or the reporting of... .... Experience in research programming preferred. Knowledge about clinical trials a plus. Ability to perform effectively in team environment...SASWork experience placement
$40 - $60 per hour
Overview Statistical Programmer job at Planet Group. Seattle, WA. Responsibilities Accountable for... ...the pharmaceutical, biotechnology or clinical research industry. Proven experience using statistical software packages SAS and R. Strong understanding of statistical...SASRemote workcny15,000 - cny25,000 per month
...documentation. 2. Develop, validate and maintain SAS programs for data analysis, reporting... ...and ADaM, to ensure compliance with clinical data submission standards. 3. For... ...and applications. 7. Assist senior SAS programmers in completing various types of clinical...SASFull time- Join to apply for the Statistical Programmer role at Katalyst CRO Overview Join to apply for... ...role at Katalyst CRO . Responsibilities The SAS/Statistical Programmer will also be... ...ensuring the accuracy and consistency of clinical data. The successful candidate will work...SASContract work
- ...rapidly, and we are currently seeking a full-time, office-based SAS Programmer to join our Biostatistics team. This position will work on a... ...Medpace Overview Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV...SASFull timeContract workWork at officeLocal areaImmediate startFlexible hours
- Overview Senior SAS Programmer job at cGxPServe. Washington DC. Responsibilities The Senior SAS Programmer will be responsible for statistical programming for the client's clinical studies. In this role, you will develop and validate SAS programs for data presentation,...SASWork experience placement
- ...Sciences Company, needs to hire a Statistical Programmer to provide programming support for Phase... ...ownership. Works collaboratively with Clinical Operations, Clinical Data Management,... ...pharmaceutical or health related industry. Advanced SAS programming skill s and experience in...SAS
